Patient attitudes and preferences about expanded noninvasive prenatal testing

por Dubois, Marie-Line, Winters, Patricia D., Rodrigue, Marc-André, Gekas, Jean
Publicado 2023

Use of cell-free signals as biomarkers for early and easy prediction of preeclampsia

por Gekas, Jean, Boomer, Theresa Hopkins, Rodrigue, Marc-André, Jinnett, Kristine N., Bhatt, Sucheta
Publicado 2023

Comparison of different strategies in prenatal screening for Down’s syndrome: cost effectiveness analysis of computer simulation

por Gekas, Jean, Gagné, Geneviève, Bujold, Emmanuel, Douillard, Daniel, Forest, Jean-Claude, Reinharz, Daniel, Rousseau, François
Publicado 2009

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma

por Gekas, Jean, Langlois, Sylvie, Ravitsky, Vardit, Audibert, François, van den Berg, David-Gradus, Haidar, Hazar, Rousseau, François
Publicado 2014

Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues

por Gekas, Jean, Langlois, Sylvie, Ravitsky, Vardit, Audibert, François, van den Berg, David Gradus, Haidar, Hazar, Rousseau, François
Publicado 2016

Myoblasts Derived From Normal hESCs and Dystrophic hiPSCs Efficiently Fuse With Existing Muscle Fibers Following Transplantation

por Goudenege, Sébastien, Lebel, Carl, Huot, Nicolas B, Dufour, Christine, Fujii, Isao, Gekas, Jean, Rousseau, Joël, Tremblay, Jacques P
Publicado 2012

Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities

por Gekas, Jean, van den Berg, David-Gradus, Durand, Audrey, Vallée, Maud, Wildschut, Hajo Izaäk Johannes, Bujold, Emmanuel, Forest, Jean-Claude, Rousseau, François, Reinharz, Daniel
Publicado 2011

Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes

por Mossfield, Tamara, Soster, Erica, Menezes, Melody, Agenbag, Gloudi, Dubois, Marie-Line, Gekas, Jean, Hardy, Tristan, Jurkowska, Monika, Kleinfinger, Pascale, Loggenberg, Kelly, Marchili, Pablo, Sirica, Roberto
Publicado 2022

Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study

por Rousseau, François, Langlois, Sylvie, Johnson, Jo-Ann, Gekas, Jean, Bujold, Emmanuel, Audibert, François, Walker, Mark, Giroux, Sylvie, Caron, André, Clément, Valérie, Blais, Jonatan, MacLeod, Tina, Moore, Richard, Gauthier, Julie, Jouan, Loubna, Laporte, Alexandre, Diallo, Ousmane, Parker, Jeremy, Swanson, Lucas, Zhao, Yongjun, Labelle, Yves, Giguère, Yves, Forest, Jean-Claude, Little, Julian, Karsan, Aly, Rouleau, Guy
Publicado 2019

A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study

por Lapointe, Julie, Dorval, Michel, Chiquette, Jocelyne, Joly, Yann, Guertin, Jason Robert, Laberge, Maude, Gekas, Jean, Hébert, Johanne, Pomey, Marie-Pascale, Cruz-Marino, Tania, Touhami, Omar, Blanchet Saint-Pierre, Arnaud, Gagnon, Sylvain, Bouchard, Karine, Rhéaume, Josée, Boisvert, Karine, Brousseau, Claire, Castonguay, Lysanne, Fortier, Sylvain, Gosselin, Isabelle, Lachapelle, Philippe, Lavoie, Sabrina, Poirier, Brigitte, Renaud, Marie-Claude, Ruizmangas, Maria-Gabriela, Sebastianelli, Alexandra, Roy, Stéphane, Côté, Madeleine, Racine, Marie-Michelle, Roy, Marie-Claude, Côté, Nathalie, Brisson, Carmen, Charette, Nelson, Faucher, Valérie, Leblanc, Josianne, Dubeau, Marie-Ève, Plante, Marie, Desbiens, Christine, Beaumont, Martin, Simard, Jacques, Nabi, Hermann
Publicado 2021